AU629109B2 - Tenidap as an inhibitor of the release of elastage by neutrophils - Google Patents
Tenidap as an inhibitor of the release of elastage by neutrophils Download PDFInfo
- Publication number
- AU629109B2 AU629109B2 AU73586/91A AU7358691A AU629109B2 AU 629109 B2 AU629109 B2 AU 629109B2 AU 73586/91 A AU73586/91 A AU 73586/91A AU 7358691 A AU7358691 A AU 7358691A AU 629109 B2 AU629109 B2 AU 629109B2
- Authority
- AU
- Australia
- Prior art keywords
- tenidap
- elastase
- mammal
- neutrophils
- pharmaceutically
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Reproductive Health (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Plant Substances (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US495888 | 1990-03-19 | ||
US07/495,888 US5006547A (en) | 1990-03-19 | 1990-03-19 | Tenidap as an inhibitor of the release of elastase by neutrophils |
Publications (2)
Publication Number | Publication Date |
---|---|
AU7358691A AU7358691A (en) | 1992-08-06 |
AU629109B2 true AU629109B2 (en) | 1992-09-24 |
Family
ID=23970396
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU73586/91A Ceased AU629109B2 (en) | 1990-03-19 | 1991-03-18 | Tenidap as an inhibitor of the release of elastage by neutrophils |
Country Status (17)
Country | Link |
---|---|
US (1) | US5006547A (de) |
EP (1) | EP0448261B1 (de) |
JP (1) | JPH0678230B2 (de) |
KR (1) | KR960016511B1 (de) |
AT (1) | ATE133071T1 (de) |
AU (1) | AU629109B2 (de) |
CA (1) | CA2038410C (de) |
DE (1) | DE69116404T2 (de) |
DK (1) | DK0448261T3 (de) |
HU (1) | HU212492B (de) |
IE (1) | IE70732B1 (de) |
IL (1) | IL97520A (de) |
MY (1) | MY107227A (de) |
NZ (1) | NZ237450A (de) |
PH (1) | PH27229A (de) |
PT (1) | PT97062B (de) |
ZA (1) | ZA911980B (de) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5008283A (en) * | 1990-03-19 | 1991-04-16 | Pfizer Inc. | Use of tenidap to inhibit activation of collagenase and to inhibit the activity of myeloperoxidase |
US5122534A (en) * | 1991-02-08 | 1992-06-16 | Pfizer Inc. | Use of tenidap to reduce total serum cholesterol, ldl cholesterol and triglycerides |
US5545656A (en) * | 1995-04-05 | 1996-08-13 | Pfizer Inc. | 2-Oxidole-1-carboxamide pharmaceutical agents for the treatment of alzheimer's disease |
US6544556B1 (en) | 2000-09-11 | 2003-04-08 | Andrx Corporation | Pharmaceutical formulations containing a non-steroidal antiinflammatory drug and a proton pump inhibitor |
EP1390062A4 (de) * | 2001-05-02 | 2005-09-14 | Blood Res Center | Modulatoren der elastase-inhibitor-sekretion |
CA2657606A1 (en) | 2006-03-08 | 2007-09-13 | Cortria Corporation | Combination therapy with non-selective cox inhibitors to prevent cox-related gastric injuries |
EP2886541A1 (de) * | 2013-12-19 | 2015-06-24 | Sanofi | Oxindolderivate, ihre Herstellung und ihre therapeutische Verwendung zur Behandlung von durch AMPK vermittelten Erkrankungen |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4556672A (en) * | 1984-03-19 | 1985-12-03 | Pfizer Inc. | 3-Substituted 2-oxindole-1-carboxamides as analgesic and anti-inflammatory agents |
US4678802A (en) * | 1985-07-09 | 1987-07-07 | Pfizer Inc. | 1-acylcarbamoyloxindole-3-carboxamides as antiinflammatory agents |
US5036099A (en) * | 1987-02-02 | 1991-07-30 | Pfizer Inc. | Anhydrous, crystalline sodium salt of 5-chloro-3-(2-thenoyl)-2-oxindole-1-carboxamide |
DE3852145T2 (de) * | 1987-02-18 | 1995-04-06 | Beecham Group Plc | Indolderivate, Verfahren zu deren Herstellung und pharmazeutische Präparate, die diese enthalten. |
US4861794A (en) * | 1988-04-13 | 1989-08-29 | Pfizer Inc. | 3-substituted-2-oxindole-1-carboxamides as inhibitors of interleukin-1 biosynthesis |
US4853409A (en) * | 1988-04-13 | 1989-08-01 | Pfizer Inc. | 3-substituted-2-oxindole-1-carboxamides for suppressing T-cell function |
DE3814504A1 (de) * | 1988-04-29 | 1989-11-09 | Bayer Ag | (alpha)-substituierte 4-(chinolin-2-yl-methoxy)phenylessigsaeuren und -ester, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
-
1990
- 1990-03-19 US US07/495,888 patent/US5006547A/en not_active Expired - Lifetime
-
1991
- 1991-03-08 EP EP91301963A patent/EP0448261B1/de not_active Expired - Lifetime
- 1991-03-08 DE DE69116404T patent/DE69116404T2/de not_active Expired - Fee Related
- 1991-03-08 DK DK91301963.4T patent/DK0448261T3/da active
- 1991-03-08 PH PH42109A patent/PH27229A/en unknown
- 1991-03-08 AT AT91301963T patent/ATE133071T1/de not_active IP Right Cessation
- 1991-03-12 IL IL9752091A patent/IL97520A/en not_active IP Right Cessation
- 1991-03-15 IE IE86191A patent/IE70732B1/en not_active IP Right Cessation
- 1991-03-15 NZ NZ237450A patent/NZ237450A/en unknown
- 1991-03-15 CA CA002038410A patent/CA2038410C/en not_active Expired - Fee Related
- 1991-03-18 HU HU91871A patent/HU212492B/hu not_active IP Right Cessation
- 1991-03-18 MY MYPI91000439A patent/MY107227A/en unknown
- 1991-03-18 KR KR1019910004237A patent/KR960016511B1/ko not_active IP Right Cessation
- 1991-03-18 AU AU73586/91A patent/AU629109B2/en not_active Ceased
- 1991-03-18 ZA ZA911980A patent/ZA911980B/xx unknown
- 1991-03-18 PT PT97062A patent/PT97062B/pt not_active IP Right Cessation
- 1991-03-19 JP JP3130751A patent/JPH0678230B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
PH27229A (en) | 1993-05-04 |
KR960016511B1 (ko) | 1996-12-14 |
EP0448261B1 (de) | 1996-01-17 |
DE69116404D1 (de) | 1996-02-29 |
IE910861A1 (en) | 1991-09-25 |
PT97062B (pt) | 1998-07-31 |
IL97520A (en) | 1995-12-31 |
HUT60622A (en) | 1992-10-28 |
AU7358691A (en) | 1992-08-06 |
EP0448261A2 (de) | 1991-09-25 |
CA2038410C (en) | 1995-01-24 |
MY107227A (en) | 1995-10-31 |
ATE133071T1 (de) | 1996-02-15 |
US5006547A (en) | 1991-04-09 |
EP0448261A3 (en) | 1992-04-08 |
PT97062A (pt) | 1991-10-31 |
DK0448261T3 (da) | 1996-02-12 |
NZ237450A (en) | 1997-02-24 |
JPH04234814A (ja) | 1992-08-24 |
JPH0678230B2 (ja) | 1994-10-05 |
IE70732B1 (en) | 1996-12-11 |
HU212492B (en) | 1996-07-29 |
IL97520A0 (en) | 1992-06-21 |
KR910016327A (ko) | 1991-11-05 |
HU910871D0 (en) | 1991-09-30 |
DE69116404T2 (de) | 1996-05-30 |
ZA911980B (en) | 1992-10-28 |
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Publication | Publication Date | Title |
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AU629109B2 (en) | Tenidap as an inhibitor of the release of elastage by neutrophils | |
EP0337628B1 (de) | 3-Substituierte 2-Oxindol-1-carboxamid-Derivate zur Hemmung der Aktivität der T-Zellen | |
AU637745B2 (en) | Use of tenidap to inhibit the activity of myeloperoxidase | |
AU601325B2 (en) | 3-substituted-2-oxindole-1-carboxamides as inhibitors of interleukin-1 biosynthesis | |
AU630580B2 (en) | Use of tenidap to reduce total serum cholesterol, ldl cholesterol and triglycerides | |
EP0543855A1 (de) | Verwendung von arylhydroxyharnstoffverbindungen zur behandlung von atherosklerose | |
CORREIA et al. | Severe acute form of adult dermatomyositis treated with cyclosporine | |
US5192790A (en) | 3-substituted-2-oxindole derivatives as inhibitors of interleukin-1 biosynthesis | |
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Miyamoto et al. | The effects of R-75,317 on antiglomerular basement membrane glomerulonephritis in rats | |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |